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Titel: 
VerfasserIn: 
Sonst. Personen: 
Sprache/n: 
Englisch
Veröffentlichungsangabe: 
Dordrecht : Springer Netherlands, 1986
Umfang: 
Online-Ressource : online resource
Bibliogr. Zusammenhang: 
Erscheint auch als (Druck-Ausgabe) : ISBN 9789401083171
Erscheint auch als (Druck-Ausgabe) : ISBN 9780412268908
Erscheint auch als (Druck-Ausgabe) : ISBN 9789400940963
Erscheint auch als (Druck-Ausgabe) : ISBN 9789402419603
ISBN: 
978-94-009-4095-6
Weitere Ausgaben: 978-94-010-8317-1 (Druckausgabe)
Identifier: 
Mehr zum Titel: 
1 Introduction2 Isolation and culture -- 2.1 Introduction -- 2.2 Choice of starting material -- 2.3 Enzymes and osmotica -- 2.4 Isolation methods -- 2.5 Purification of isolated protoplasts -- 2.6 Protoplast viability and plating density -- 2.7 Methods for protoplast culture -- 2.8 Cell wall regeneration -- 2.9 Division and growth -- 2.10 Isolation of subprotoplasts -- 2.11 Conclusions -- References -- 3 Regeneration of plants -- 3.1 History of plant regeneration studies -- 3.2 Organogenesis -- 3.3 Embryogenesis -- 3.4 Handling of regenerated plantlets -- 3.5 Genetic stability of regenerated plantlets -- References -- 4 Protoplast fusion -- 4.1 Introduction -- 4.2 Methods to induce fusion -- 4.3 Selection of fusion hybrids -- 4.4 Which plants to hybridize -- 4.5 Cybrid formation -- 4.6 Conclusions -- References -- 5 Protoplasts as physiological tools -- 5.1 Studies on DNA, RNA and protein synthesis -- 5.2 Protoplasts for isolation of cell components -- 5.3 Protoplasts for studies on cell wall regeneration -- References -- 6 Uptake of foreign materials -- 6.1 Introduction -- 6.2 Nuclei and subprotoplasts -- 6.3 Chloroplasts and mitochondria -- 6.4 Bacteria -- 6.5 Blue-green algae -- 6.6 Viruses -- 6.7 DNA -- 6.8 Non-biological materials -- References -- 7 Genetic engineering -- 7.1 Introduction -- 7.2 Induced tumours -- 7.3 The infective plasmid -- 7.4 Transformation of protoplasts -- 7.5 Which genes to engineer? -- References.
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Klassifikation der Library of Congress: Q1-390
Dewey Dezimal-Klassifikation: 50; ; 300; ; 001.3;
Book Industry Communication: GT
bisacsh: SCI000000
Inhalt: 
1 Introduction -- 2 Isolation and culture -- 2.1 Introduction -- 2.2 Choice of starting material -- 2.3 Enzymes and osmotica -- 2.4 Isolation methods -- 2.5 Purification of isolated protoplasts -- 2.6 Protoplast viability and plating density -- 2.7 Methods for protoplast culture -- 2.8 Cell wall regeneration -- 2.9 Division and growth -- 2.10 Isolation of subprotoplasts -- 2.11 Conclusions -- References -- 3 Regeneration of plants -- 3.1 History of plant regeneration studies -- 3.2 Organogenesis -- 3.3 Embryogenesis -- 3.4 Handling of regenerated plantlets -- 3.5 Genetic stability of regenerated plantlets -- References -- 4 Protoplast fusion -- 4.1 Introduction -- 4.2 Methods to induce fusion -- 4.3 Selection of fusion hybrids -- 4.4 Which plants to hybridize -- 4.5 Cybrid formation -- 4.6 Conclusions -- References -- 5 Protoplasts as physiological tools -- 5.1 Studies on DNA, RNA and protein synthesis -- 5.2 Protoplasts for isolation of cell components -- 5.3 Protoplasts for studies on cell wall regeneration -- References -- 6 Uptake of foreign materials -- 6.1 Introduction -- 6.2 Nuclei and subprotoplasts -- 6.3 Chloroplasts and mitochondria -- 6.4 Bacteria -- 6.5 Blue-green algae -- 6.6 Viruses -- 6.7 DNA -- 6.8 Non-biological materials -- References -- 7 Genetic engineering -- 7.1 Introduction -- 7.2 Induced tumours -- 7.3 The infective plasmid -- 7.4 Transformation of protoplasts -- 7.5 Which genes to engineer? -- References.
Isolated plant protoplasts are 'naked' cells that have had their cell wall removed either by mechanical action or by enzymic digestion. As a result of wall removal the only barrier that exists between the cell protoplasm and the external environment is the plasma membrane. The removal of the cell wall has drastic osmotic consequences for the isolated cell. Rather like animal cells, the isolated protoplasts must be maintained in an osmotically balanced (isotonic) nutrient medium or they will burst. As will be seen later, the isolation of plant protoplasts is not a particularly new event; as early as the 1890s scientists were isolating protoplasts mechanically and studying effects such as protoplast streaming. What has brought protoplast technology to the forefront of plant biology is the potential application of these structures in non-traditional plant improvement methods. Extreme care must be exercised by the reader, however, in be­ lieving some of the claims that have been put forward for the use of protoplasts in improvement programmes. In the 20 years since the first experiments in routine enzyme isolation of large numbers of protoplasts no real improvement has been obtained in a commercial crop plant. This does not mean that improvement is impossible; it simply indicates that it may be a longer term objective than some people would like to admit.
 
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